Bernice E. Morrow

Biochemistry, Genetics and Molecular BiologyMedicineAgricultural and Biological Sciences

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 21 papers. Top paper: “Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States”.

Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States

Genes(2021)10.3390/genes12071030

N/A

0.250DataRank · unranked

4 citations

Fadi I. Musfee, Laura E. Mitchell, Elizabeth Goldmuntz, Hongbo M. Xie, Håkon Håkonarson +7 more

scDAPP: a comprehensive single-cell transcriptomics analysis pipeline optimized for cross-group comparison

NAR Genomics and Bioinformatics(2024)10.1093/nargab/lqae134

N/A

0.173DataRank · unranked

2 citations

Xiang Yu Zheng, Kevyn Jackson, Bang H. Hoang, Bernice E. Morrow, Deyou Zheng +1 more

Single cell multi-omic analysis identifies a Tbx1 -dependent multilineage primed population in the murine cardiopharyngeal mesoderm

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.12.24.424342

N/A

0DataRank · unranked

0 citations

Yang Liu, Christopher De Bono, Dario Righelli, Andrea Cirino, Wei Wang +10 more

Single cell multi-omic analysis identifies a Tbx1-dependent multilineage primed population in murine cardiopharyngeal mesoderm

Nature Communications(2021)10.1038/s41467-021-26966-6

N/A

0DataRank · unranked

57 citations

Yang Liu, Christopher De Bono, Dario Righelli, Andrea Cirino, Wei Wang +12 more

Crk and Crkl have shared functions in neural crest cells for cardiac outflow tract septation and vascular smooth muscle differentiation

Human Molecular Genetics(2021)10.1093/hmg/ddab313

N/A

0DataRank · unranked

7 citations

Silvia E. Racedo, Alexander Diacou, Tae‐Ju Park, Bin Zhou, Bernice E. Morrow +1 more

Common Variation in Cytoskeletal Genes Is Associated with Conotruncal Heart Defects

Genes(2021)10.3390/genes12050655

N/A

0DataRank · unranked

3 citations

A. J. Agopian, Elizabeth Goldmuntz, Håkon Håkonarson, Bernice E. Morrow, Deanne Taylor +5 more

Platelet findings in 22q11.2 deletion syndrome correlate with disease manifestations but do not correlate with GPIb surface expression

Clinical Genetics(2022)10.1111/cge.14227

N/A

0DataRank · unranked

9 citations

T. Blaine Crowley, Chintan Jobaliya, Alice Bailey, Daniel E. McGinn, Kimberly Gaiser +10 more

Influence of Parent-of-Origin on Intellectual Outcomes in the Chromosome 22q11.2 Deletion Syndrome

Genes(2022)10.3390/genes13101800

N/A

0DataRank · unranked

4 citations

T. Blaine Crowley, Tracy Heung, Oanh Tran, Edward Moss, Elaine H. Zackai +7 more

Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS and sporadic congenital heart disease

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.09.30.507111

N/A

0DataRank · unranked

0 citations

Yujue Wang, Lijie Shi, Donna M. McDonald‐McGinn, T. Blaine Crowley, Daniel E. McGinn +45 more

An optimized approach for multiplexing single-nuclear ATAC-seq using oligonucleotide conjugated antibodies

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.12.22.521637

N/A

0DataRank · unranked

0 citations

Taylor V. Thompson, Eric Sosa, Hiroko Nomaru, David M. Reynolds, Robert Dubin +6 more

Single-cell transcriptomics uncovers a non-autonomous Tbx1-dependent genetic program controlling cardiac neural crest cell development

Nature Communications(2023)10.1038/s41467-023-37015-9

N/A

0DataRank · unranked

39 citations

Yang Liu, Alexander Ferrena, Aneesa Valentine, Deyou Zheng, Bernice E. Morrow +1 more

Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS

npj Genomic Medicine(2023)10.1038/s41525-023-00363-y

N/A

0DataRank · unranked

12 citations

Yujue Wang, Lijie Shi, Donna M. McDonald‐McGinn, T. Blaine Crowley, Daniel E. McGinn +47 more

Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia

Molecular Psychiatry(2023)10.1038/s41380-023-02009-y

N/A

0DataRank · unranked

5 citations

Yingjie Zhao, M. Reza Jabalameli, Nha Nguyen, Joydeep Mitra, Ann Swillen +15 more

An optimized approach for multiplexing single-nuclear ATAC-seq using oligonucleotide-conjugated antibodies

Epigenetics & Chromatin(2023)10.1186/s13072-023-00486-7

N/A

0DataRank · unranked

4 citations

Taylor V. Thompson, Eric Sosa, Hiroko Nomaru, David M. Reynolds, Robert Dubin +6 more

Dgcr8 functions in the secondary heart field for outflow tract and right ventricle development in mammals

Developmental Biology(2023)10.1016/j.ydbio.2023.12.005

N/A

0DataRank · unranked

4 citations

Yang Liu, Lijie Shi, Deyou Zheng, Bernice E. Morrow, Silvia E. Racedo

Risk of meningomyelocele mediated by the common 22q11.2 deletion

Science(2024)10.1126/science.adl1624

N/A

0DataRank · unranked

21 citations

Sangmoon Lee, Kit Sing Au, T. Blaine Crowley, Valeria Capra, Meade Haller +74 more

scDAPP: a comprehensive single-cell transcriptomics analysis pipeline optimized for cross-group comparison

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.05.06.592708

N/A

0DataRank · unranked

1 citations

Xiang Yu Zheng, Kevyn Jackson, Bang H. Hoang, Bernice E. Morrow, Deyou Zheng +1 more

Prevalence and spectrum of congenital heart disease in individuals with distal chromosome 22q11.22-23 deletions

medRxiv(2025)10.1101/2025.10.15.25337915

N/A

0DataRank · unranked

0 citations

Daniel E. McGinn, T. Blaine Crowley, Lydia Rockart, Audrey Green, Victoria Giunta +18 more

Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion

Molecular Psychiatry(2020)10.1038/s41380-020-0654-3

N/A

0DataRank · unranked

136 citations

Worrawat Engchuan, Matthew S. Hestand, Tracy Heung, Aaron M. Holleman, H. Richard Johnston +95 more

Prevalence and Spectrum of Congenital Heart Disease in Individuals With Distal Chromosome 22q11.22–23 Deletions

Clinical Genetics(2025)10.1111/cge.70118

N/A

0DataRank · unranked

0 citations

Daniel E. McGinn, T. Blaine Crowley, Lydia Rockart, Audrey Green, Victoria Giunta +18 more

Optical mapping of the 22q11.2DS region reveals complex repeat structures and preferred locations for non-allelic homologous recombination (NAHR)

Scientific Reports(2020)10.1038/s41598-020-69134-4

N/A

0DataRank · unranked

34 citations

Oanh Tran, Andrea Jin, Danielle Carrado, Benjamin A. Silva, Lahari Uppuluri +13 more